FDAFebruary 22, 2024device

RELAY PRO Thoracic Stent-Graft System, containing one endovascular stent-graft system, IFU, and patient tracking card, sterile: (a) Part number 28-M4-34-100-34U; (b) Part number 28-M4-30-095-30U; (c) Part number 28-M4-46-155-46U; (d) Part number 28-M4-32-155-32S; (e) Part number 28-M4-36-250-32S;...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The stent-graft inside the delivery system was the incorrect size.

What to do

FDA enforcement status: Completed

Brands named

bolton medicalbolton

UPCs

843576149656843576149632843576149847843576100183843576100763843576100572843576100343843576100114843576100824843576100954843576100831843576101449

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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